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Fda and otc drugs, how to treat tinnitus with drugs - .

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Whenever you use an over-the-counter (OTC) medicine, reading the drug product's labeling is important for taking care of yourself and your family. In the Federal Register of March 1999, the Food and Drug Administration published the OTC Drug Facts Label regulation. Before simplifying the OTC label, the FDA conducted extensive research on how consumers use OTC drug product labels. Previously, information about product directions, warnings, and approved uses appeared in different places on the label depending on the OTC product and brand. Patterned after the Nutrition Facts food label, the Drug Facts label uses simple language and an easy-to-read format to help people compare and select OTC medicines and follow dosage instructions. Specific warnings, including when the product should not be used under any circumstances, and when it is appropriate to consult with a doctor or pharmacist.

Along with the standardized format, the label uses plain-speaking terms to describe the facts about each OTC drug. If you read an OTC medicine label and still have questions about the product, talk to your doctor, pharmacist, or other health care professional.
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The label tells you what the medicine is supposed to do, who should or shouldn't take it, and how to use it.
This regulation required most OTC drug products to comply with the new format and content requirements by May 2002. One major problem has been the readability of the labels, especially for older Americans, who purchase almost 30 percent of the OTC drugs sold in the United States.

Finding information about inactive ingredients has also been a challenge for those who may be allergic to an ingredient in a drug product. This section also describes side effects that could occur and substances or activities to avoid.
The labeling of OTC medicines has always contained usage and safety information for consumers. The label also requires a type size large enough to be easily read and specific layout details--bullets, spacing between lines, and clearly marked sections--to improve readability.

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Comments to “Fda and otc drugs”

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  2. Arzu_18:
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